Canonical Allele Identifier: CA1118986159
Gene: PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1169315425
gnomAD v3: 8-127079862-C-T
gnomAD v4: 8-127079862-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079862C>T , CM000670.2:g.127079862C>T GRCh38
NC_000008.10:g.128092107C>T , CM000670.1:g.128092107C>T GRCh37
NC_000008.9:g.128161289C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-729G>A
Search 100 bp 5'
Search 100 bp 3'